Ecological surveillance of bat coronaviruses in Sarawak, Malaysian Borneo

Objective Coronaviruses (CoVs) are natural commensals of bats. Two subgenera, namely Sarbecoviruses and Merbecoviruses have a high zoonotic potential and have been associated with three separate spillover events in the past 2 decades, making surveillance of bat-CoVs crucial for the prevention of the next epidemic. The study was aimed to elucidate the presence of coronavirus in fresh bat guano sampled from Wind Cave Nature Reserve (WCNR) in Sarawak, Malaysian Borneo. Samples collected were placed into viral transport medium, transported on ice within the collection day, and preserved at − 80 °C. Nucleic acid was extracted using the column method and screened using consensus PCR primers targeting the RNA-dependent RNA polymerase (RdRp) gene. Amplicons were sequenced bidirectionally using the Sanger method. Phylogenetic tree with maximum-likelihood bootstrap and Bayesian posterior probability were constructed. Results CoV-RNA was detected in ten specimens (47.6%, n  = 21). Six alphacoronavirus and four betacoronaviruses were identified. The bat-CoVs can be phylogenetically grouped into four novel clades which are closely related to Decacovirus-1 and Decacovirus-2, Sarbecovirus, and an unclassified CoV. CoVs lineages unique to the Island of Borneo were discovered in Sarawak, Malaysia, with one of them closely related to Sarbecovirus. All of them are distant from currently known human coronaviruses.

HCoV-OC43 and HCoV-HKU1) in which nearly all of them can be traced to their bat origin [1,2]. The discovery of two bats CoVs, KSA-287 from Taphozous perforatus and RaTG13 from Rhinolophus affinis with 100% and 96% sequence identity to MERS-CoV and SARS-CoV-2 respectively, sealed the hypothesis that these CoVs of Public Health Emergency of International Importance (PHEIC) indeed have originated from bats. However, the progenitor for SARS-CoV was never discovered.
The SARS-CoV epidemic started in Guangdong, China in 2002, rampaging through numerous countries for nine months, infecting 8096, claiming the lives of 774. A decade later, MERS-CoV emerged in the Kingdom of Saudi Arabia, but cases have mostly been reported around the Middle East, Africa and South Asia with occasional exported cases [3]. As of June 2021, there were 2564 confirmed cases of MERS, including 886 associated death, with the case-fatality-rate (CFR) of 34.4% [4]. Later, a novel beta-coronavirus named SARS-CoV-2 was discovered in a cluster of patients with acute viral pneumonia of unknown origin in Wuhan, China. However, SARS-CoV-2 has a relatively low CFR of 2.1% compared to SARS-CoV and MERS-CoV but due to its high transmissibility, it has resulted in more than 208 million infections and 4.4 million deaths worldwide (as of 17th August 2021) [5].

BMC Research Notes
Bats from the order Chiroptera, including microbat families Rhinolophidae, Hipposideridae, Emballonuridae, Miniopteridae, and Vespertilionidae are known to be the reservoir of bat CoVs in Asia [2]. These competent hosts can also be found in the touristic Wind Cave Nature Reserve (WCNR) in Bau District, Sarawak, Malaysian Borneo [6].
Other virological surveillance in Sarawak, Malaysia mainly revolves around viruses of public health importance, but the study on bat viruses in Gunung Mulu National Park, Sarawak (4°02′60.00′′ N 114°55′58.80′′ E), has led to the identification of Sarawak mobatvirus, a novel hantavirus within the genus mobatvirus [7]. Therefore, in the wake of the COVID-19 pandemic, it is timely that virological surveillance should be conducted to determine the presence and diversity of bat-CoVs in bat populations in Sarawak.

Main text
Methods WCNR is located 1º24′55′′ N 110º08′7′′ E (Fig. 1). We have collected 21 pooled bat guano from WCNR on March 8th, 2021 and screened them for the presence of the partial RNA-dependent RNA polymerase gene of coronavirus. Five (5) pellets of fresh guano from insectivorous bats collected on a plastic tarp were pooled in 500 μL of ice-cold viral transport medium (1st Base), vortex-mixed and centrifuged at 13,000×g at 4 °C. Supernatant was used for nucleic acid extraction using High Pure Viral Nucleic Acid Extraction Kit (Roche). For phylogenetic analysis, the 440-bp gene of coronavirus was amplified using family-wide hemi-nested RT-PCR using the modified Watanabe primers: CoV-RVS3 5′-CCA TCA TCASWYR AAT CAT CAT A-3′, CoV-FWD3 5′-GGT TGG GAY TAY CCHAAR TGT GA-3′ and CoV-FWD4/Bat 5′-GAY TAY CCHAAR TGT GAY AGA GC-3′. The complementary DNA synthesis was performed at 42 °C for 60 min using RevertAid Reverse Transcriptase (Ther-moScientific) using CoV-RVS3. The conditions for the first round PCR were 2 min at 94 °C; 40 cycles for 20 s at 94 °C, 30 s at 50 °C, 30 s at 72 °C; 1 min. The conditions for the nested-PCR are identical except for the higher annealing temperature at 59 °C. PCR amplicons were resolved in 2% agarose buffered in 1X TBE (1st Base) supplemented with 10 μg/mL ethidium bromide (Promega), excised, and sequenced using the BigDye terminator v3.0. Amplicons were sequenced bidirectional using CoV-FWD3 and CoV-FWD4/Bat, amplicons with mixed or poor sequence read were ligated into pJet2.1 vector and transformed into chemically competent Escherichia coli DH5α (ThermoScientific) and sequenced using the vector primers (1st Base) [8]. Amplicon sequences were analysed with the Basic Local Alignment Search Tool software (BLAST) at the National Centre for Biotechnology Information (NCBI) to determine their corresponding species followed by nucleotide identity analysis using Sequence Identity and Similarity (SIAS) (http:// imed. med. ucm. es/ Tools/ sias. html).

Discussion
Despite the small sample size, the findings from this study confirm the presence of CoVs in nearly half of the bat guano sampled in WCNR, Sarawak, Malaysia. This supports the argument that bat guano is a good surrogate for Bat CoV surveillance without the need for life animal capture [10].
All of these CoVs were highly related to CoVs that were previously found in Hipposideros spp. suggesting that Hipposideros could potentially be their preferred natural host, but these viruses were also found in other bat species such as Rhinolophus, Miniopterus, Taphozous, Myotis, Scotophilus, and Cynopterus (fruit bats) [11][12][13][14]. However, SARS-CoV-2 related viruses were mainly identified in Rhinolophus bats such as R. affinis and R. malayanus in Yunnan, China, R. shameli in Northern Cambodia and R. acuminatus in Eastern Thailand [15].
Of the four novel clades, Borneo Beta-1 is probably of a greater concern as two members from its sister clade are responsible for two pandemics within the past two decades. Nonetheless, Borneo Beta-1 viruses are found to be distant to the SARS-CoVr-2 RaTG13 (MN996532) (69.1-69.7% nt identity), the proposed progenitor of the pandemic SARS-CoV-2 identified in Rhinolophus affinis [16]. Further investigations to determine its receptor use should be carried out to assess the risk of spillover from bats to humans [17].
Caves are haven for ecotourism but may also serve as hotspots for bat CoV zoonosis since other sympatric wildlife is present and physical contact with viruscontaminated guano is nearly unavoidable. Although it is widely accepted that an intermediary host is almost always required for efficient spillover of Bat CoV to humans [18,19], the discovery of CoV strain RaTG13 in Mojiang, Yunnan, China where fatal SARS-like epidemic in 2012 did not discount the possibility of direct spillover [20]. Following three CoVs zoonoses in the past 2 decades, ecotourism and research pertaining to caves and bats should be revisited.
There have been no records of bat CoV zoonoses in Sarawak. Nevertheless, it is important to note that clinical diagnostics of potential SARS-like/Influenza-like respiratory diseases in Sarawak had historically involved only bacterial diagnosis [21]. Virological surveillances were rarely carried out except through external research collaboration that would not impact patient care. Despite the record adoption of real-time molecular assays in the healthcare settings during the SARS-CoV-2 pandemic, it was also shown that real-time assay was inferior to pan-CoV assay in the detection of seasonal HCoV, missing out on many positives, including the novel canine-CoVs in the human respiratory specimens [22,23]. This is not surprising as real-time primers and probes tend to be more specific as compared to the degenerate primers used in most pan-CoV assays that increased the probability of detecting all circulating CoV genera. Do bear in mind that primer designs are largely based on the skewed representation of viral sequences obtained from other geographical locations, disregarding on the dispersal and vicariance phenomenon. To this, all SARS-like illnesses should be screened using the pan-CoV assay in hope of identifying the potential spillover rapidly and stop the epidemic at the source in a timely manner.

Conclusions
The bats in WCNR harbour rich diversity of both alphacoronaviruses and beta-coronaviruses that are unique to Borneo Island. Although these novel CoVs are not closely related to any seasonal, epidemic, and pandemic CoVs; visitors that are at risk of being in direct contact with virus contaminated guano. Basic biosafety precautions should be practised to minimize the possibility of spillover.

Limitations
The study was based on a small sample size obtained in a restrictive condition during the SARS-CoV-2 pandemic. Increasing the sample size may potentially lead to the discovery of more novel CoVs or quasispecies of the CoVs reported in this study. The partial RdRp sequence analysis may have suggested the novelty of the CoVs discovered in this study but longer sequence information on other genes and hopefully whole genomic sequences may enhance the current findings or suggest otherwise.